Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000179.2 | 338 | Silent Mutation | CGA,CGC | R62R | NP_000170.1 |
NM_001281492.1 | 338 | Silent Mutation | CGA,CGC | R62R | NP_001268421.1 |
NM_001281493.1 | 338 | UTR 5 | NP_001268422.1 | ||
NM_001281494.1 | 338 | Intron | NP_001268423.1 | ||
XM_011532798.1 | 338 | Intron | XP_011531100.1 | ||
XM_011532799.1 | 338 | Intron | XP_011531101.1 |